Magdalena N. Georgieva1*
Charles K. Paull2
Crispin T. S. Little3Mary McGann4
Diana Sahy5Daniel Condon5Lonny Lundsten2Jack Pewsey3
David W. Caress2
Robert C. Vrijenhoek2- 1Department of Life Sciences, Natural History Museum, London, United Kingdom
- 2Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States
- 3School of Earth and Environment, University of Leeds, Leeds, United Kingdom
- 4United States Geological Survey, Menlo Park, CA, United States
- 5NERC Isotope Geosciences Laboratory, British Geological Survey, Keyworth, United Kingdom
Multibeam bathymetric mapping of the Santa Monica Basin in the eastern Pacific has revealed the existence of a number of elevated bathymetric features, or mounds, harboring cold seep communities. During 2013–2014, mounds at ∼600 m water depth were observed for the first time and sampled by Monterey Bay Aquarium Research Institute’s ROV Doc Ricketts. Active cold seeps were found, but surprisingly one of these mounds was characterized by massive deposits composed of fossil serpulid worm tubes (Annelida: Serpulidae) exhibiting various states of mineralization by authigenic carbonate. No living serpulids with equivalent tube morphologies were found at the site; hence the mound was termed “Fossil Hill.” In the present study, the identity of the fossil serpulids and associated fossil community, the ages of fossils and authigenic carbonates, the formation of the fossil serpulid aggregation, and the geological structure of the mound are explored. Results indicate that the tubes were most likely made by a deep-sea serpulid lineage, with radiocarbon dating suggesting that they have a very recent origin during the Late Pleistocene, specifically to the Last Glacial Maximum ∼20,000 years ago. Additional U-Th analyses of authigenic carbonates mostly corroborate the radiocarbon dates, and also indicate that seepage was occurring while the tubes were being formed. We also document similar, older deposits along the approximate trajectory of the San Pedro Basin Fault. We suggest that the serpulid tube facies formed in situ, and that the vast aggregation of these tubes at Fossil Hill is likely due to a combination of optimal physical environmental conditions and chemosynthetic production, which may have been particularly intense as a result of sea-level lowstand during the Last Glacial Maximum.
Introduction
Cold seeps are remarkable marine environments characterized by the effluence of near ambient-temperature reduced fluids, usually rich in methane or hydrogen sulfide, from the seafloor. In recent years, information from autonomous underwater vehicle (AUV) surveys has greatly aided the discovery of cold seeps in the deep sea, which are recognized by the presence of patches of irregular bathymetry in areas of otherwise undifferentiated sediment (Hovland and Judd, 1988; MacDonald et al., 2003; Wagner et al., 2013; Paull et al., 2015). Cold seeps often manifest as topographic mounds, pockmarks and outcrops of authigenic carbonates (Wagner et al., 2013), and are renowned for the often vast chemosynthesis-supported biological productivity that occurs at these sites compared to the otherwise generally food-limited deep sea. Cold seeps are also known to have been important habitats for deep-sea fauna throughout Earth’s history since at least the Paleozoic (Peckmann et al., 1999b; Barbieri et al., 2004), and today, siboglinid tubeworms (Annelida), bathymodiolin mussels and vesicomyid clams (Bivalvia) thrive at seeps (Kiel, 2010), because they host chemoautotrophic endosymbionts that obtain nutrients from seeping fluids (Dubilier et al., 2008). The elevated productivity of cold seeps also provides habitats for a wealth of additional organisms that have not yet been found to possess such symbionts, such as fish, brachyuran crabs, polynoids, and serpulid tubeworms. The latter (Annelida: Serpulidae) are remarkable for their ability to form vast reef-like aggregations in shallow marine and brackish waters. While serpulids can occur in large numbers at deep-sea seeps (Olu et al., 1996a,b; Levin et al., 2012; Amon et al., 2017), they rarely construct sizeable reef structures below the photic zone. Here, we report on the discovery of, and investigations into, an unusually large accumulation of fossil serpulids within deep-sea waters that occurs in association with an active cold seep.
Serpulid worms are common in all marine environments, occurring from the intertidal down to hadal depths (Ippolitov et al., 2014), and possess an anterior end that terminates in a fan-like structure (crown) used for suspension-feeding (Kupriyanova et al., 2006). These annelids are easily recognized by their dwelling tubes, which are comprised of calcium carbonate and typically secured to a hard substrate. Members of this family are also notable for their gregarious behavior, amassing to form vast reefs by using the tubes of conspecifics as settlement substrate (ten Hove and van den Hurk, 1993). These worms can hence function as important ecosystem engineers, altering local hydrodynamics, and providing habitat structure utilized by other marine organisms (Schwindt et al., 2001), but can also accumulate to foul marine structures and modify ecosystems within which they are invasive. Large serpulid aggregations or reefs are commonly found in enclosed embayments of normal salinity or in brackish estuaries or lagoons (Bianchi et al., 1995). Conditions such as reduced competition for food and space, reduced predation, larval retention and possibly also high primary production are considered to promote reef formation behavior by serpulids, under which they can form reefs reaching tens of square meters in extent and over one meter in thickness (ten Hove and van den Hurk, 1993; Bianchi et al., 1995; Hoeksema and ten Hove, 2011). Although rare, there are also reports of serpulid reefs from deeper waters, such as serpulid-coral aggregations that were observed at depths of 450–650 m in the Adriatic Sea (Sanfilippo et al., 2013). In 1999, the discovery of an extensive reef comprised almost exclusively of the species Serpula narconensis at 91–105 m depth off the South Georgia continental shelf was reported, from where a single trawl collected over 1.5 tons of tubes made by this species (Ramos and San Martín, 1999). Serpulids have also been found to occur in high abundance within deep-sea cold seep environments (Vinn et al., 2013, 2014). Species of Laminatubus sp. are present in large numbers at the hydrothermal seeps of Jaco Scar on the Costa Rica convergent margin (Levin et al., 2012), and other serpulid species at cold seeps off northern Peru (Olu et al., 1996a), at the Barbados Accretionary Prism (Olu et al., 1996b) where they gather at high densities on concretions around mussel beds, and at seeps off Trinidad and Tobago (Amon et al., 2017). Within cold seeps, large serpulid populations are likely sustained by filter-feeding on the greater concentrations of organic matter in the water column at these sites, and have not yet been reported to possess microbial epi- or endo-symbionts.
Serpulid build-ups are also known from the fossil record, dating back to the Late Triassic (ten Hove and van den Hurk, 1993). One of the most extensive fossil serpulid reefs occurs at the Triassic-Lias boundary in southern Spain, in which a unit comprised mainly of tubes of the species Filograna socialis outcrops for 75 m and reaches 25 m in thickness. This reef is reported to have formed in deep water, but still within the photic zone (Braga and Lopez-Lopez, 1989). Large aggregations of tubes preserved in several fossil cold seep deposits have also been ascribed to the serpulids, such as the tube fossils of the Cretaceous Sada limestone (Nobuhara et al., 2008) and the Miocene Ca’ Fornace and Marmorito carbonates of northern Italy (C.T.S. Little pers. obs.; Peckmann et al., 1999a; Kiel et al., 2018). In the Sada limestone deposit, the maximum observed thickness of the serpulid facies is greater than 6 m (Nobuhara et al., 2016). The identification of the serpulid species comprising fossil reefs can be problematic as the systematics of extant serpulids is based mainly on characteristics associated with the animals (Ippolitov et al., 2014). Nevertheless, a number of tube characteristics can be helpful such as tube aggregation, coiling/curving, attachment to substrate and external sculpture (see Ippolitov et al., 2014). Increasingly the ultrastructure of tubes is also used in relating fossil to recent taxa, in cases where the tube walls of fossil serpulids have not been significantly diagenetically altered (Vinn, 2005, 2008; Taylor and Vinn, 2006; Vinn et al., 2008a).
Multibeam bathymetric mapping of the Santa Monica Basin, southern California, has helped to reveal the existence of a number of elevated bathymetric features, or mounds, harboring cold seep communities (Normark et al., 2003; Hein et al., 2006). Exploration of these mounds using AUV-based 1-m resolution mapping and subbottom profiling, followed by ROV exploration and sampling, has revealed the presence of sub-surface gas hydrates. Paull et al. (2008) have hypothesized hydrate formation as a mechanism for mound uplift, while the proximity of some of the mounds to the trajectory of the San Pedro Basin fault system (Ryan et al., 2012) suggests that their formation may be associated with fault activity (Fisher et al., 2003; Gardner et al., 2003). During 2013–2014 Monterey Bay Aquarium Research Institute (MBARI) expeditions, an additional mound that had not previously been explored by remotely operated vehicle (ROV) was observed to be comprised predominantly of a large number of fossil serpulid tubes exhibiting various states of mineralization by authigenic carbonate. The mound was hence termed “Fossil Hill.” In this study, results of extensive exploration of this enigmatic mound are presented with the aim to characterize the physical and biological features of this anomalous structure, as well as to ascertain its mode of formation, and whether this is associated with fluid seepage.
Materials and Methods
Seafloor Mapping and Sample Collection
High-resolution mapping and sub-bottom profiling surveys of selected topographic features within the Santa Monica Basin region were conducted in March 2013 using an AUV equipped with 400 kHz Reson 7125 multibeam sonar, 110 kHz chirp sidescan sonar, and a 1–6 kHz sweep chirp subbottom profiler (see Caress et al. (2008) for further methodological details). An objective was to explore along the inferred trace of the San Pedro Basin fault looking for the morphologies indicative of seafloor seepage sites (Paull et al., 2015), and evidence of recent movements along the fault (Ryan et al., 2012). AUV dives 20133006m1 and 20130311m1 revealed areas of anomalously rough seafloor both south or north of Santa Monica Canyon respectively, Fossil Hill being one of these (Figure 1). These areas were further explored during two ROV diving cruises of the R/V Western Flyer in May 2013 and June 2014. The AUV survey of the Fossil Hill site was repeated in April 2018 (AUV dive 201807m1) following improvement in processing software.
Figure 1. Location and bathymetry of Fossil Hill. (A) Map of California showing the location of the Santa Monica Bay area, red box shows area pictured in B. (B) Santa Monica Bay showing the location of Fossil Hill (red box, pictured in detail in C) in relation to the Santa Monica canyon and the approximate position of the San Pedro Basin fault (SPBF, dashed black line; Ryan et al., 2012). The location of the sampling site northeast of Fossil Hill (DR631) is also shown. (C) Detailed bathymetry of the Fossil Hill mound. Blue and green lines show the tracks of the elevation profiles in Figure 6. The black dots within these tracks represent individual vibracore locations, with start, and end vibracore numbers labeled. Red box shows area in which video-mosaic (Figure 3) was performed. Black star denotes the location of an extensive live clam and bacterial mat bed, and a large pockmark (27 m wide, 4 m deep) on the northern margin is indicated with an arrow. The sampling site southeast of Fossil Hill (DR630) is labeled.
Samples were obtained from the Fossil Hill mound, as well as nearby seafloor exhibiting similar topography along the approximate axis of the San Pedro Basin Fault (Figure 1). Sample collection from these sites took place during seven dives of the ROV Doc Ricketts; DR476 and DR626-631 (Supplementary Table S1). The manipulator arms of the ROV were used to collect more heavily mineralized rock samples, while loose tube and bivalve shell rubble, as well as living bivalves, were collected using an ROV operated scoop and through push-coring (up to 22 cm long). A vibracorer mounted to the ROV was used to collect up to 165 cm long cores in areas of soft sediment. Push cores were extruded on board the ship, and all rock and fossil samples were subsequently rinsed in fresh water and dried, while live bivalves were preserved in 80% ethanol. Vibracores were logged, split, photographed and preserved at the United States Geological Survey, Menlo Park, CA, United States. Supplementary Figure S1 shows locations of rock, vibracore, and push-core sampling at Fossil Hill. Video footage from a systematic ROV flight during DR627 was used to construct a video mosaic of a sub-region of the Fossil Hill mound (Figure 1). During this dive, the ROV was maintained ∼1 m above the seabed in order to collect multiple, overlapping parallel sweeps of video footage over the region of interest. Still images were later extracted from the video footage, and loaded into PhotoScan Pro (v. 1.1.6, Agisoft LLC) to build the mosaic.
Fossil Identification
Fossil serpulid tubes were photographed and imaged in greater detail using an Olympus SZH10 stereomicroscope. Five fragments of tubes from a range of diameters were also imaged using a Hitachi S-3400N-II variable pressure scanning electron microscope (SEM) at Moss Landing Marine Laboratories, CA, United States. Transverse and longitudinal broken surfaces of the tubes were mounted onto SEM stubs, gold coated, and observed using both secondary and backscatter electrons. The composition of four tube fragments was analyzed using fourier transform infrared spectroscopy (FTIR) to determine the form of calcium carbonate present in the tubes. Tubes were ground to a powder to incorporate material from all layers, and analyzed at Imperial College London, United Kingdom, in attenuated total reflectance mode. Additional fossil taxa associated with the fossil serpulid tubes were examined using a combination of light and scanning electron microscopy, using an FEI Quanta 650 FEG-ESEM at the University of Leeds, Leeds, United Kingdom. Identifications of associated taxa to the lowest possible taxonomic level were used to create a presence-absence matrix based on their occurrence within non-vibracore samples. Several non-parametric species richness estimators such as the incidence-based coverage estimator (ICE; Lee and Chao, 1994), and the iChao2 richness estimator; Chiu et al., 2014) were calculated using R (R Core Team, 2014; Chao et al., 2015). Authigenic carbonates from a subset of rock specimens were also prepared as thin sections to observe carbonate petrography.
Dating of Fossil Fauna and Authigenic Carbonates
Eight tube and bivalve fragments not cemented by methane-derived authigenic carbonates (MDAC, Paull et al., 1992) were selected for radiocarbon analysis. These were cleaned to ensure removal of attached debris and mineralization using the following technique: cleaning using paintbrush and fresh water, placement in an ultrasonic bath for 5 min, suspension in weak hydrochloric acid (0.25 N HCl) for 2 min, placement in distilled water in an ultrasonic bath for 5 min, drying in an oven at 50°C for ∼1 h. Radiocarbon measurements were obtained by accelerator mass spectrometry (AMS) at the National Ocean Sciences Accelerator Mass Spectrometry (NOSAMS) facility, Woods Hole Oceanographic Institution, MA, United States. The radiocarbon ages were obtained by a 14C/12C ratio using a 14C half-life of 5,568 years (Stuiver and Polach, 1977). The raw radiocarbon ages were then converted to calibrated calendar ages (cal yr B.P.) using the CALIB 7.1 program (Stuiver et al., 2018). The calibrated ages are reported as the peak probability ages and the 2 sigma ranges are also included (Table 1). A reservoir age of 1750 year was applied to the worm tubes and mollusks following Mix et al. (1999) because they occupied the same substrate as bottom-dwelling (benthic) foraminifera.
Table 1. Radiocarbon (14C) dates of Fossil Hill bivalve shells and serpulid tubes.
The above cleaning steps were performed to minimize any effect of old carbon from seepage fluids on radiocarbon dates (Paull et al., 1989; Pohlman et al., 2011), while for samples affected by obvious MDAC mineralization, U-Th dating was used in order to eliminate any age bias from old carbon. MDAC cements present on the outer walls of serpulid tubes and bivalve shells, as well as infilling serpulid tubes, were dated using this technique at facilities at the NERC Geochronology and Tracers Facility, British Geological Survey, United Kingdom, following the analytical protocol outlined by Crémière et al. (2016). Additional carbon (∂13C) and oxygen (∂18O) isotope measurements conducted at the above facility were also used to confirm whether Fossil Hill carbonates are methane-derived (Supplementary Table S2).
Age interpretation of U-Th isotope data from MDAC requires a correction for the amount of initial 230Th incorporated into the carbonate either via the inclusion of detrital material or through adsorption of Th from the decay of dissolved U in the water column onto particle surfaces. In order to determine a site-specific correction for Fossil Hill, the U-Th composition of five sediment samples from four vibracores collected during dive DR630 was analyzed. Unfortunately, the sediment samples proved unsuitable for the purpose of determining an initial 230Th correction, as their measured (234U/238U) activity ratios were greater than 1, indicating the presence of young CaCO3 of either biogenic or authigenic origin. Instead, the initial 230Th correction used for the Fossil Hill MDAC was interpolated for a water depth of 650 m based on U-Th measurements of carbonate-free sediment samples from Baltimore Canyon (ca. 400 m depth) and Norfolk Canyon (ca. 1600 m depth) on the US Atlantic margin (Prouty et al., 2016). All U-Th data are listed in (Supplementary Table S3), with a selection of dates considered accurate presented in Table 2.
Table 2. U-Th composition and age interpretation of Fossil Hill methane-derived authigenic carbonate (MDAC) samples and shells and tubes.
Results
Characteristics of Fossil Hill and Associated Carbonate Deposits
The AUV surveys reveal that Fossil Hill has a lobate shape which is approximately 500 m long and 270 m at its widest extent (Figure 1C). Fossil Hill is positioned on seafloor which gently slopes to the south-west with the highest elevation reaching 622 m depth, and extending down slope to 672 m depth. The surface of Fossil Hill is 5–15 m higher than the surrounding seafloor with an overall uneven appearance, punctuated by discrete circular depressions and topographic highs. The roughly circular depressions range from a few meters to 27 m in diameter, the latter being a ∼4 m deep sinkhole or pockmark which occurs on the northern margin of Fossil Hill (Figure 1C, arrowed). The circular topographic highs are less than 50 m in diameter and up to 6 m high. The seafloor lineation that is interpreted as the approximate trace of the San Pedro Basin fault (Ryan et al., 2012) runs very close (∼50 m) to the eastern edge of Fossil Hill (Figure 1B). Sub-bottom chirp profiles across both Fossil Hill and the site 290 m to the southeast show a strong seafloor reflection where the carbonate rocks are exposed on the seafloor. Fossil Hill is positioned on top of a ridge-like tectonic feature (Figure 2), and appears to have formed on the eroded crest of this ridge where accumulating sediment was thin or absent. A thin drape of sediment seems to have covered the northern and southern ends of Fossil Hill, while reflectors passing under the deposit indicate that it is less than 5 m thick (Figures 2A–A’,D–D’). On the flanks of Fossil Hill, the strong reflector dives into the subsurface and is onlapped by a package of finely layered reflectors that are up to 45 m thick (Figures 2C–C’). This geometry reveals that the Fossil Hill deposit and the southeastern outcrop continue into the subsurface.
Figure 2. Chirp profiles taken across the Fossil Hill main mound structure. Colored insert shows the locations of the paths of profiles A–A’, B–B’, C–C’, D–D’, E–E’. The locations of recent fault offsets (red arrows), sediment drape covering or lapping onto the mound (orange arrows), and artifacts associated with a multiple reflection off the sea surface (gray arrows) are shown.
The ROV surveys show that large slabs or blocks of carbonate rock are exposed between areas of sediment drape on the surface of Fossil Hill (Figure 3). The carbonate rocks are separated by cracks and gullies, and holes at the bases of these reveal >10 cm high open cavities underneath the slabs (Figure 3). The large pockmark to the north of Fossil Hill (Figure 1C) is rimmed by large flattened carbonate slabs that at multiple locations are sloping into the crater (Figure 4A), and the crater floor is littered with boulders that appear to be a former carapace that has fallen into the depression. Neither gas bubbles or gas hydrates were observed during the ROV explorations.
Figure 3. Video-mosaic of a section of Fossil Hill (area shown in Figure 1C). White arrow head shows locations of the depression with overhang figured in more detail in Figure 4E, scale bar is approximately 2 m.
Figure 4. Characteristics of Fossil Hill. (A) Large carbonate slabs on the edge of large pockmark structure (Figure 1C) which appear to be sliding into the hole (hole is to the left in the image). (B) Carbonate rock recovered south of the main Fossil Hill mound containing many preserved bivalves, sample DR630 R-3, and scale bar is 20 mm. (C) Fossil Hill carbonate with embedded worm tubes, sample DR629 R-2, and scale bar is 20 mm. (D) Densely packed and aligned tube fragments that are only weakly cemented by carbonate, DR626 R-4, and scale bar is 20 mm. (E) Mosaic of the wall of a small depression pictured in Figure 3, showing interlayered fossil worm tubes and bivalve shells. Perspective of F (white arrow), large bivalve shells (yellow arrow), and smaller living bivalves (red arrow) are highlighted. (F) Detail of the fossil worm tubes from the depression in E (white arrow), showing that they are only weakly cemented together and are aligned in parallel. Red munidopsid squat lobsters were common. (G) Slope on the southern side of Fossil Hill littered with tube and bivalve hash.
The majority of samples of authigenic carbonate rock from Fossil Hill contained fossil serpulid worm tubes as well as bivalve and gastropod shells (Figures 4B–D and Supplementary Table S1), held together with variable amounts of carbonate cement comprised of isopachous fibrous aragonite (Figure 5). Most rock samples primarily contained worm tubes. The worm tube-dominated samples exhibited variable degrees of cementation, ranging between rock exhibiting many tubes filled with carbonate cement and strongly cemented together (Figure 4C) to weakly cemented tubes (Figure 4D). Tubes within rock samples also exhibited altering orientations, at times being mostly aligned in parallel (Figures 4D,F). Bivalve and gastropod shells rarely dominated carbonate rock faunal content (Figure 4B). The authigenic carbonate cements comprised a variable proportion of dark micrite, sometimes with distinct peloids (Figure 5A), and isopachous fibrous aragonite, often growing into open spaces within serpulid tubes and articulated bivalve shells (Figures 5A,B). In these cases the micritic cements obviously formed before the aragonite cements. In some serpulid worm tube-rich samples, they occurred as geopetal structures, indicating the tubes were horizontal to the palaeo-seafloor while they were being mineralized and after the death of the worms forming them. This was evident in the orientation of some the tubes in Figure 4F. Many of the carbonate rock samples were heavily corroded (e.g., Figures 4B,C) and had a chalky texture. Further, some had iron and manganese-rich crusts on the surfaces exposed to seawater, indicating they had been present on the seafloor for a considerable period of time. In addition, encrusting organisms were present on some of the samples, including bryozoans (Schizoporella species), small serpulids and sponges.
Figure 5. Petrographic thin section images of Fossil Hill seep carbonates. (A) Isopachous fibrous aragonite cement (ifa) and peloidal micritic sediment (ps) forming geopetal fill within shelter cavity formed by articulated vesicomyid bivalve shell (bs), plain polarized light, sample DR630 R-3, and scale bar is 200 μm. (B) Detail of isopachous fibrous aragonite crystals, plain polarized light, sample DR629 R-5, and scale bar is 80 μm.
A worm tube-rich deposit was especially evident within one of the depressions encountered with the ROV (Figures 3, 4E), in which a large proportion of the walls were exclusively built up of loose worm tubes aligned in parallel to each other (Figure 4F). These tubes were positioned on top of a layer of large bivalve shells with a shell length of up to 100 mm, while the base of the depression contained smaller, living bivalves with a shell length of up to 48 mm (Figure 4E, see section “Taxa Associated With the Fossil Serpulids”). Worm tube and bivalve shell rubble was also found to be eroding from these loosely consolidated deposits, and to be flowing down slopes (Figure 4G) as well as collecting within depressions. Vibracores collected in areas of soft sediment on Fossil Hill revealed that in some areas, depths of over 1 m of tube rubble had accumulated (Figure 6 and (Supplementary Table S1) which were generally overlain by bivalve shell rubble, however tubes and bivalves were mixed together in a number of the cores. While the tubes were very abundant throughout Fossil Hill, no live animals were found within the tubes and no live bivalves with a shell length of up to 100 mm and pictured in Figure 4E were observed. Living bivalves (shell length of up to 48 mm) were abundant at Fossil Hill, occurring in depressions between carbonate slabs (Figure 4E), and colonizing an extensive patch at high densities at which they were also overgrown by bacterial mats (location shown in Figure 1). Subsequent morphological and molecular investigations showed that the living bivalves are predominantly the vesicomyid species Ectenagena elongata. Indications of the local reworking of the Fossil Hill deposit, and the presence of living bivalves in depressions (e.g., Figure 4E), appear to disrupt stratigraphic order at the site, and hence make it difficult to derive age relationships from stratigraphy.
Figure 6. Elevation profiles through parts of Fossil Hill along which vibracores were collected, and contents of cores (78 mm diameter) collected along the above profiles. Annotations on cores show core depths in meters, and sediment refers to fine-grained hemipelagic sediment. Tracks along which elevation profiles were created are illustrated in Figure 1C.
Two other regions identified as elevated areas of rough topography in the 1-m bathymetric grids lying along the axis of the San Pedro Basin Fault were also visited during ROV dives DR630 and DR631 (Figure 1). They were found to have similar deposits consisting of fossilized serpulid tubes, bivalves and gastropods entombed within authigenic carbonates. The first (visited on ROV dive DR630) is a ∼5 m outcrop with >1 m of relief in 660 m water depth, located 290 m to the southeast of Fossil Hill on the flanks of the ridge (Figure 1C). The other (DR631) is within a ∼1.6 km long and >350 m wide area located 7.9 km northwest of Fossil Hill on the north side of Santa Monica Canyon in 509–530 m water depths, and lying on the extension of the same ridge (Figure 1B). The carbonate rock samples from these two sites generally contained fewer serpulid tubes and much less authigenic aragonite cement than the Fossil Hill samples, with these cements forming thin veins within often siliciclastic-rich micrites. The exposed surfaces of many of the DR630 and DR631 samples were heavily corroded and bored by Polydora sp. annelid worms. They were often also encrusted by bryozoans (including Haywardipora cf. orbicula and Schizoporella species), small serpulids, hydroids and sponges. These are all indications of long seafloor exposure.
Fossil Hill Paleo-Community
Fossil Serpulid Tubes
No complete worm tubes were found, however, the lack of diagenetic alteration of many of the Fossil Hill tube fragments enabled their morphology to be assessed in detail. The tubes either occurred singly, or more commonly as two or more attached to each other along a longitudinal edge (Figures 7A,B). The majority of fragments were straight with only occasional strongly sinuous tubes observed (Figures 7A,B) and were generally circular or near-circular in cross-section. The tubes ranged from 1 to 7 mm in diameter (mean = 3.5 mm, n = 219; (Supplementary Table S1), very small tubes up to 1 mm in diameter were occasionally observed, and several were found attached to larger tubes (Figure 7C). The outer tube walls exhibited a texture of closely spaced, fine transverse wrinkles or growth-lines, that were more obvious in a subset of the tubes, and also appeared to be present in the tube layer below the outermost (Figure 7D). Many of the tubes also contained a single distinct undulating keel on their outer surfaces (Figures 7A,E), as well as peristomes, or occasional thickenings of short transverse sections of the tube wall (Figure 7F). Intricate ribbed calcareous tabulae were also found inside a subset of the tubes (Figure 7G). The above morphological characteristics were generally shared across the majority of tube fragments observed from Fossil Hill.
Figure 7. Morphology of Fossil Hill serpulid tubes. (A) Several attached tube fragments with keels (white arrows) showing gregarious growth, sample DR476 A-1, and scale bar is 10 mm. (B) Curved nature of some of the fragments, sample DR629 PSC-52, and scale bar is 10 mm. (C) Small tube attached to larger tube, sample DR626 PSC-66, and scale bar is 2 mm. (D) Detail of transverse wrinkles apparent on some outer tube surfaces which are also present in the tube layer beneath the outermost, sample DR476 A-1, and scale bar is 1 mm. (E) Detail of tube keels, sample DR476 A-1, and scale bar is 1 mm. (F) Detail of peristomes occasionally present on the tubes (white arrows), sample DR476 A-1, and scale bar is 1 mm. (G) Detail of a tabula inside one of the tubes, sample DR476 A-1, and scale bar is 1 mm.
Analysis of the ultrastructure of the tubes (Figure 8) revealed them to be comprised of two distinct layers – a fine-grained inner layer and a coarser-grained outer layer (Figure 8A). The innermost tube layer was composed of acicular crystallites approximately 5 μm in length, arranged in multiple orientations and known in serpulid tubes as an irregularly oriented prismatic (IOP) tube ultrastructure (Figure 8B). This texture continued further into the tube wall, where it was partially mixed with homogeneous carbonate cement (Figure 8C), or was in patches replaced by a grainy texture that is either primarily comprised of homogeneous cement, or is a recrystallized version of the irregularly oriented prismatic texture in Figures 8B,C. Longitudinal sections of tubes also revealed that the irregularly oriented prismatic texture was more intact toward the inside of the tube wall, and becomes increasingly homogeneous in nature toward the outer tube wall (Figure 8E). The crystals of the outer tube wall are approximately 25–30 μm in length and represent a spherulitic prismatic structure (SPHP) (Figure 8F). Comparison to established FTIR spectra for calcite and aragonite as well as mixtures of the two forms (Loftus et al., 2015) revealed that the Fossil Hill serpulid tubes to be predominantly comprised of calcite (based on the absence of a double peak at the 711 and 700 cm-1 wavelength positions; see Supplementary Figure S2).
Figure 8. Ultrastructure of Fossil Hill tubes. (A) Transverse section of a tube showing fine-grained inner layer and coarse-grained outer layer, sample DR476 A-1, and scale bar is 50 μm. Arrow shows perspective of B, and boxes show representative locations for the textures pictured in C, D, and F. (B) View looking down onto the inner tube surface showing irregularly oriented prismatic (IOP) ultrastructure comprised of crystallites approximately 5 μm in length, sample DR626 R-4, and scale bar is 20 μm. (C) Detail of inner tube layer in transverse section showing IOP ultrastructure with homogeneous cement, sample DR626 R-4, and scale bar is 10 μm. (D) Detail of outer part of fine-grained tube layer showing a grainy appearance, sample DR626 R-4, and scale bar is 5 μm. (E) Fine-grained inner tube layer in transverse section showing a transition from a prismatic structure to a grainy/platy structure from left to right, sample DR629 BB, and scale bar is 15 μm. (F) Detail of outer coarse-grained tube layer showing spherulitic prismatic (SPHP) ultrastructure, sample DR626 R-4, and scale bar is 10 μm.
We interpret all of the tubes as belonging to the same species, as significant differences between them were not observed (smaller differences could be due to intraspecific variation and the observed presence of a range of ontogenic stages), and as dense serpulid settlement is often dominated by a single taxon. The long, straight sections of the Fossil Hill serpulid tube fragments are typical of dense settlement of these annelids, which often results in tubes growing in an upright position away from their settlement substrate and leads to parallel erect tube morphologies (ten Hove, 1979). Gregarious behavior and reef formation is commonly observed in serpulid genera such as Hydroides, Ficopomatus, and Serpula, all of which are known from the eastern Pacific (Bastida-Zavala, 2008), however, generally not from deep waters. The size of the Fossil Hill tubes is consistent with those made by Serpula and Protula, however Serpula tubes commonly have funnel-shaped peristomes (Ippolitov et al., 2014; Figures 2F,G) which were not observed on any of the Fossil Hill tubes, and Protula tubes from the region do not have peristomes (Reish and Mason, 2003). The species Serpula columbiana is described from the west coast of North America and thus locally to Fossil Hill, but S. columbiana tubes also notably lack the longitudinal keels observed on the Fossil Hill tubes (Kupriyanova, 1999). In addition, the ultrastructure of the tubes of three Serpula species examined by Vinn et al. (2008b) does not match that of the Fossil Hill tubes.
Deep-sea serpulid genera include Bathyvermilia, Neovermilia and Laminatubus, and the occurrence of the Fossil Hill tubes in deep water, their presence in great numbers, as well as and the undulating keel observed on the larger tube fragments from Fossil Hill, are features more consistent with genera such as Neovermilia and Laminatubus which can also have similar keels and can occur in vast numbers at deep-sea sites of organic enrichment (E. Kupriyanova pers. comm.). The tube ultrastructure presented by the Fossil Hill tubes of an inner IOP layer and an outer SPHP layer, as well as their calcite composition, is also observed in Laminatubus alvini tubes (ten Hove and Zibrowius, 1986). The latter species is described from eastern Pacific hydrothermal vents and can have substantial unattached tube portions with a circular cross-section, however, comparison of these sections with those of Fossil Hill tubes revealed differences in the smoothness of the outer tube wall, as well as degree of undulation of the keels. Neovermilia has not yet been documented from the above region, although there is some similarity in tube ultrastructure (Vinn et al., 2008b). There is also very little information on the occurrence of tabulae in the tubes of modern serpulid species from the genera mentioned above. These “floors” inside serpulid tubes form in response to damage of the posterior tube ending, and are likely produced through the pygidium of the serpulid worm acting as a mold for carbonate precipitation (Hedley, 1958). Tabulae could thus potentially be formed by a variety of serpulids, and their morphology can be somewhat variable even within a species, thus diminishing their utility taxonomically. Based on the above considerations, the morphology and ultrastructure of the Fossil Hill serpulid tubes is most consistent with the deep-sea genus Laminatubus, and we therefore give them the tentative identification of ?Laminatubus. The tubes may indeed belong to a now extinct species despite their recent age, or the conditions which led to such a large proliferation of these serpulids may have produced particular tube morphotypes that have not yet been observed in extant species.
Taxa Associated With the Fossil Serpulids
Many of the Fossil Hill samples contained dead benthic mollusk shells in addition to the serpulid tubes (Supplementary Table S4). E. elongata was the most common of these associated mollusks, and many specimens in the vibracores (Figure 6) and also as rubble on slopes (Figure 4G) appeared relatively fresh, with remaining periostracum and a lack of overgrowing authigenic carbonate cement, indicating they were relatively young amongst the rest of the samples (see section “Ages of Fossil Hill Faunas and Authigenic Carbonates”). Other specimens of E. elongata in the rock samples were worn and chalky, indicating a greater age. Other bivalve taxa in the Fossil Hill samples included species that are known or strongly suspected to host sulfide-oxidizing chemosymbionts in live specimens. These were the solemyid Acharax johnsoni (Figure 9I), the vesicomyids Archivesica packardana (Figures 3B, 9C), Phreagena soyoae (=P. kilmeri jr. syn.) (Figures 4E, 9A) and Pliocardia stearnsii, the lucinid Lucinoma aequizonata (Figure 9D), and the thyasirids Thyasira flexuosa (Figure 9E) and Axinopsida serricata (Figure 9F). The vesicomyid taxa are all known from methane seep sites further north in Monterey Bay (e.g., Goffredi and Barry, 2002; Johnson et al., 2016). The other bivalve taxa are typical of deep-sea fauna in the East Pacific: the pectinid Delectopecten vancouverensis (Figure 9H) and the nuculid Nucula carlottensis (Figure 9G; Coan et al., 2000).
Figure 9. Images of representative bivalves and gastropods from Fossil Hill samples. (A) Phreagena soyoae, right valve external view, DR627 Bio-2 clam scoop, and scale bar is 10 mm. (B) Ectenagena elongata, right valve external view, DR626 A-1, and scale bar is 10 mm. (C) Archivesica packardana, right valve external view, DR626 A-1, and scale bar is 10 mm. (D) Lucinoma aequizonata, right valve external view, DR629 PSC-61, and scale bar is 10 mm. (E) Thyasira flexuosa, right valve external view, DR627 (BB), and scale bar is 5 mm. (F) Axinopsida serricata, right valve internal view, DR627 R-2, SEM, and scale bar is 1 mm. (G) Nucula carlottensis, left valve external view, DR627 R-2, SEM, and scale bar is 1 mm. (H) Delectopecten vancouverensis, right valve external view, DR627 BB, SEM, and scale bar is 0.5 mm. (I) Acharax johnsoni, partial left valve external view, DR627 BIO-2, and scale bar is 10 mm. (J) Depressigyra sp. apertural view, DR476 A-1, and scale bar is 1 mm. (K) Provanna laevis, apertural view, DR476 A-1, SEM, and scale bar is 1 mm. (L) Provanna lomana, apertural view, DR476 A-1, SEM, and scale bar is 1 mm. (M) Provanna sp., adapertural view, DR476 A-1, SEM, and scale bar is 1 mm. (N) Puncturella rothi, apical view, DR627 R-2, SEM, and scale bar is 1 mm. (O) Puncturella rothi, lateral view, DR628 R-3, and scale bar is 2 mm. (P,Q) Paralepetopsis sp., apical (P) and lateral (Q) views, DR627 R-2, and scale bars are 1 mm. (R,S) Pyropelta “low-spired,” anterior (R) and lateral (S) views, DR627 R-2, and scale bars are 1 mm. (T) Pyropelta corymba, lateral view, DR627 R-2, and scale bar is 1 mm. (U) Lepetodrilus sp., lateral view, DR629 R-2, and scale bar is 2 mm.
The benthic gastropods in the Fossil Hill samples (Supplementary Table S4) are a mixture of taxa occurring at other methane seep sites to the north and south, including the peltospirid Depressigyra sp. (Figure 9J), the leptodrilid Lepetodrilus sp. (Figure 9U), the neolepetopsid Paralepetopsis sp. (Figures 9P,Q), the provannids Provanna laevis (Figure 9K), Provanna lomana (Figure 9L) and the pyropeltid Pyropelta corymba (Figure 9T; Warén and Bouchet, 1993; Levin et al., 2015), and Eastern Pacific deep-sea taxa: the raphitomid Pleurotomella sp. and fissurellid Puncturella rothi (Figures 9N,O; McLean, 1984). The curved shape of the apertures of many of the Paralepetopsis sp. and Pyropelta spp. specimens (Figure 9R), as well as their intimate association with the serpulid tubes in the lightly to heavily mineralized samples strongly indicates they lived on the tubes during life, probably scraping microbial mats from the tube surfaces. This tight association between worm tubes and grazing limpets has been commonly noted from modern and fossil cold seep sites (e.g., Okutani et al., 1992; Jenkins et al., 2007; Saether et al., 2012), although in these cases the tubes are those of siboglinids and not serpulids.
The mollusk taxa associated with the DR630 and DR631 samples are of lower diversity than those in the Fossil Hill samples, and are a sub-set of them (Supplementary Table S4). One exception is sample DR631 R-3, which contains specimens of the pteropod Cavolinia uncinata, which were derived from the water column and then incorporated into the authigenic carbonates as they formed within the sediments. While 24 taxa were recorded, species richness estimation based on data within Supplementary Table S4 predicted a minimum of 30–53 fossil species (ICE: 29.5; iChao2: 53.3) from Fossil Hill and associated sites.
Ages of Fossil Hill Faunas and Authigenic Carbonates
Radiocarbon measurements made on the carbonate in the walls of serpulid tubes from several locations around Fossil Hill resulted in a narrow range of calculated ages ranging between 23 and 25 cal ka BP (1000 years before present; Table 1). The δ13CV PDB values of the same samples ranged from -18.06 to -11.01‰. Thus, these Late Pleistocene radiocarbon ages should be treated as a maximum due to potential addition of old carbon effects outlined earlier. Radiocarbon dating of bivalve specimens produced an age similar to that of serpulid tubes for a specimen of P. soyoae (23 cal ka BP; Table 1), while a shell of the bivalve E. elongata was shown to be recent using this technique.
Cements occurring on fossil taxa showed very depleted δ13C signatures (Supplementary Table S2). U-Th dating of cements and fossils was largely consistent with radiocarbon dates, however, U-Th age interpretation was complicated by the fact that most ROV samples yielded a wide range of ages, spanning several tens of ka. Given the size of the samples, such age variation most likely results from some degree of open system behavior through U loss. As a result, the youngest date from each sample was assumed to be representative for the respective locality, provided that its initial (234U/238U) activity ratio was within uncertainty of the mean seawater value of 1.1468 (Andersen et al., 2010). Based on this approach we estimate the age of tube-associated authigenic carbonates recovered during dives DR626-630 to be around 17–30 ka (Table 2). The older end of this age range is underpinned by statistically equivalent data from three different samples, with only one date from DR626 indicative of a potential older age of around 43 ka. Samples recovered during dive DR631 were analyzed, but returned results consistent with open system behavior, which precluded age interpretation. U-Th dating of cements on bivalve shells from specimens collected on the northern end of Fossil Hill produced ages of approximately 7.1 ka, while carbonate cement on fossil bivalve specimens from the DR630 dive site yielded an age of 20.8 ka (Table 2).
Discussion
As serpulid tubes were observed along much of Fossil Hill’s extent of over 500 m by 250 m, this mound appears to host one of the largest known accumulations of fossil serpulids, greatly exceeding the dimensions of the Triassic-early Jurassic fossil serpulid reefs from southern Spain (Braga and Lopez-Lopez, 1989). The Fossil Hill serpulid accumulation is also unusual in being found in deep-sea waters, in association with fossil cold seep faunas, and at a site that still supports an active chemosynthetic biological community with a different assemblage of species. While many mounds characterized by active seepage have been discovered off the coast of California in deep waters (e.g., Orange et al., 2002; Paull et al., 2008, 2015), Fossil Hill and the associated exposures documented in this study are the only examples so far dominated by fossil serpulid tube facies. All of the Fossil Hill serpulid tubes analyzed through radiocarbon dating have maximum ages of 23–24 cal ka BP (Table 1) while U-Th dating suggests some tubes are over 16–30 ka old (Table 2), demonstrating that this accumulation is remarkably recent in origin and that the species responsible for the accumulation may still be extant.
The current topography of Fossil Hill (Figure 1C) appears to be largely a result of differential erosion which has exposed authigenic carbonates and vast quantities of serpulid tube fossils, and this process is likely also responsible for exposing similar facies ∼8 km to the northwest, and ∼300 m to the southeast along the same fault zone as Fossil Hill. Our data are consistent with the formation of the serpulid tube accumulation within deep-sea waters at the Fossil Hill site. This is strongly suggested by the concentrated, well-sorted and oriented nature of the Fossil Hill serpulid tube facies (Figure 4E). As only the anterior ends of the tubes were found, there appears to have been some reworking of the deposit. However, based on the considerations above, reworking has likely been spatially constrained to mostly within the Fossil Hill mound area. While Fossil Hill is located in close proximity to the base of the Santa Monica Canyon (Figure 1), the mound is situated over 500 m from the main channel in a part of the seabed unlikely to be influenced by canyon transport processes. It therefore appears unlikely that the tubes could have been transported to their current location from shallower, photic zone waters. The morphology of the Fossil Hill tubes is also more consistent with a deep-sea serpulid genus, further suggesting that they likely formed in deep water at the Fossil Hill site.
Is Formation of the Fossil Hill Serpulid Reef Linked to Seepage?
As cold seeps are renowned for supporting greater productivity in comparison to many other deep-sea environments, an apparent explanation for the occurrence of such a large colony of serpulids within a deep-sea cold seep is that its formation is related to productivity from seepage. There are clear indications that active fluid seepage existed at Fossil Hill at the time of tube formation, and may therefore have contributed to the proliferation of these annelids and thus the size of the resulting reef deposit. U-Th dating of MDAC cements on tube surfaces (Table 2), and both radiocarbon and U-Th dating of tubes (Table 1), indicate that tube formation and fluid seepage were contemporaneous at Fossil Hill during the period 20–25 cal ka BP, while dating of shells additionally suggests that the larger chemosynthetic bivalve species, Phreagena soyoae, was also living at the site during this time (Table 1). Large vesicomyid bivalves have sulfur-oxidizing bacterial symbionts and require sulfide-rich reducing environments (Krylova and Sahling, 2010), therefore it is likely that the Fossil Hill P. soyoae specimens (Figure 9A), as well as many of the other fossil fauna (section “Taxa Associated With the Fossil Serpulids”; Figures 9B–U) associated with the ?Laminatubus sp. tubes, would have relied on seeping fluids at the site for their nutrition. In addition, δ13C values for the fossil serpulid tubes (Table 1) also indicate the involvement and importance of methane within the environment at the time the serpulid tubes were forming. The δ13C values of serpulid tubes are considered to closely resemble those of the waters within which they grew. However vital effects have been reported for this group, whereby tube δ13C values are shifted to more negative values by 4–7‰ (Videtich, 1986; Lojen et al., 2014). The mechanisms leading to the above effects are however unclear, and a metabolic influence on the low δ13C values of the Fossil Hill serpulid tubes therefore cannot be ruled out.
While some U-Th measurements suggest slightly older ages for Fossil Hill ?Laminatubus sp. of 30–43 ka, most U-Th dates, as well as radiocarbon measurements on the above tubes and P. soyoae cluster at 16–25 cal ka BP (Tables 1, 2). This may indicate that a discrete event could have occurred during this time period, leading firstly to a vast proliferation of, and subsequently the local extinction of serpulids at the Fossil Hill site. The radiocarbon ages of the tubes approximately coincide with the last glacial maximum (LGM; 20 cal ka BP), during which sea-levels are estimated to have been 110–130 m lower than at present (Lambeck and Chappell, 2001; Bintanja et al., 2005). Intensity of fluid seepage is believed to vary with climatic conditions, in part because ocean warming or a lowering of pressure associated with sea-level changes can lead to dissociation of gas hydrate sequestered near the gas hydrate stability boundary (Kvenvolden, 1988; MacDonald et al., 2003; Buffett and Archer, 2004). For example, the intensity of methane seepage at cold seeps off the coast of mainland Norway and western Svalbard has been linked to isostatic rebound and pulses of sedimentation associated with glaciation during the Late Pleistocene, which altered the stability of gas hydrates (Karstens et al., 2018; Wallmann et al., 2018). Fossil Hill is now at 600 m water depth, near the top of the present methane hydrate stability zone in the Santa Monica Basin (Paull et al., 2008). However, the over 100 m sea-level drop during the LGM likely caused the methane hydrate stability conditions to shift enough for methane hydrate in near-seafloor sediments to decompose, and for methane to be released from sediments. The occurrence of pockmarks, cracks, gullies and caverns on the Fossil Hill mound could indicate the historical presence of gas hydrates that have dissociated, leaving void spaces in the strata and morphologies that suggest seafloor collapse. Methane released from the dissociation of gas hydrate inventoried within near-seafloor sediments, and linked to the LGM sea-level lowstand could have promoted heightened productivity and hence the proliferation of a serpulids as well as chemosynthetic fauna at the Fossil Hill site.
An intriguing question presented by the above scenario is why serpulids, rather than symbiont-bearing chemosynthetic fauna, would have dominated Fossil Hill during a possible period of intense methane seepage during the LGM. It is possible that the Fossil Hill ?Laminatubus sp. could have possessed chemosynthetic symbionts. While serpulids with such symbiotic associations have not yet been formally described, Laminatubus sp. from the Jaco Scar seeps have been found to possess microbial communities on their crowns, and research into the nature of their association with the worms is currently in progress (S. Goffredi, pers. comm.). The reason for the extinction of Fossil Hill ?Laminatubus sp. are however unclear. While there appears to have been active seepage at the Fossil Hill mound during 20–16 ka and 7 ka from MDAC cements (Table 2), we cannot at present determine if it was continuous, therefore the possibility exists that the serpulids may have become locally extinct at Fossil Hill during substantial periods of seepage quiescence. Indeed, the bivalve P. soyoae appears to also be locally extinct at the Fossil Hill site despite the occurrence of living populations of these species in nearby seeps (Goffredi and Barry, 2002).
Serpulid Reef Formation and Other Factors
Aspects of the physical environment such as an advantageous position along a fault scarp that provides optimal access to nutrients entrained in water currents, or an unusual composition of the seeping fluid, may also account for why a taxon not deemed to be chemosynthetic was so abundant and co-occurred with seepage at Fossil Hill. Faults can provide conduits for the migration of fluids and are known to be associated with cold seep communities (Zitter et al., 2008), and could additionally have provided serpulids with hard substrate in the form of MDAC for attachment. While other mounds off the Californian coast were generally not found to harbor large abundances of fossil serpulids, serpulid tubes similar to those of Fossil Hill were recovered at the two additional authigenic carbonate outcrops along the approximate trajectory of the San Pedro Basin Fault sampled during dives DR630 and DR631 (Figure 1). Therefore, the proximity of fossil serpulid tube facies to the San Pedro Basin Fault may indicate an association between this facies and fault activity. The subset of Fossil Hill U-Th dates that also predate the LGM could suggest that factors other than nutritional benefits from seepage productivity may have been responsible for serpulid reef growth. However, data on historical fault and water current movements are very limited, and it thus remains difficult to account for why serpulids are extinct at the Fossil Hill site today.
It is likely that the formation of the fossil serpulid reef at Fossil Hill is due to a combination of favorable environmental conditions as well as heightened productivity from seepage, particularly ∼20 ka. Serpulid populations in general are known to boom for discrete time periods under which distinct environmental conditions prevail (ten Hove and van den Hurk, 1993), which the Triassic-early Jurassic fossil serpulid reefs from southern Spain (Braga and Lopez-Lopez, 1989) as well as those found near South Georgia (Ramos and San Martín, 1999) demonstrate can occur away from coastal settings in more open, near-deep to deep-sea waters. The large extent of the Fossil Hill deposit, and the known role of serpulids as ecosystem engineers in virtue of reef construction, means that Fossil Hill likely constituted a significant deep-sea habitat for other marine fauna, with the mollusk fauna associated with Fossil Hill serpulids (and the estimated fossil species richness) attesting to this. During the time of active serpulid reef growth during the Late Pleistocene, Fossil Hill could therefore potentially be classed as an “animal forest” (Rossi, 2013; Reyes-Bonilla and Jordán-Dahlgren, 2017) in virtue of providing three-dimensional habitat complexity that can alter physical and biological characteristics of the site.
Conclusion
Detailed AUV surveys in combination with extensive ROV sampling have revealed the existence of a massive serpulid paleo-colony dominated by ∼20 cal ka BP tubeworms off southern California. The deposit also contains fossil cold seep faunas and methane-derived carbonates. Similar massive-sized deposits dominated by serpulids have not previously been documented in the deep sea. However, the proportion of the seafloor that has been explored with tools and techniques that allow features like this to be identified is still very small. Further exploration has the potential to shed insight into whether living populations of the Fossil Hill ?Laminatubus serpulids may yet still exist within the southern California region, to elucidate the relationship between these tubeworms and fluid seepage, and thus provide answers to the intriguing question as to whether these serpulids may have had chemosymbionts.
Data Availability
All datasets generated for this study are included in the manuscript and/or the Supplementary Files.
Author Contributions
Samples were collected by CP and RV, with assistance from MG. MM performed radiocarbon dating. DS and DC performed U-Th dating. DWC processed AUV data. LL provided seafloor video mosaic data. MG, CL, and JP analyzed the data and the manuscript was drafted by MG with input from CP, RV, and CL. All authors read and approved the final manuscript.
Funding
This study was provided by the David and Lucile Packard Foundation via the Monterey Bay Aquarium Research Institute. MG gratefully acknowledges funding from NERC grants NE/K500847/1 and NE/R000670/1.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We thank the crew of R/V Western Flyer, as well as the AUV and ROV Doc Ricketts pilots. We are grateful to Ivano Aiello for assistance with SEM at Moss Landing Marine Laboratories, to Hilary Sloane for assistance with stable isotope analyses, to Harry ten Hove, Elena Kupriyanova, Greg Rouse, and Olev Vinn for their advice on the identification of serpulid tubes, and Alexei Ippolitov for advice on SEM examination of serpulid tubes. We also thank Roberto Gwiazda, Esther Sumner, and Shannon Johnson for their assistance with sample collection, as well as Krystle Anderson and Eve Lundsten for their assistance with mapping data and figures. We are also grateful to Jonathan Watson and Mark Sephton for their access to and help with FTIR, to Elena Krylova, Shana Goffredi, Paul Valentich-Scott, Daniel Geiger, Anders Warén, John Taylor, Arie Janssen, and Henry Chaney for their assistance with the identification of mollusk and other taxa, and to Shannon Johnson for verification of the E. elongata identification using DNA sequences from Johnson et al. (2016), as well as additional mollusk identifications. We also thank two reviewers and Harry ten Hove for their valuable comments on the manuscript draft.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmars.2019.00115/full#supplementary-material
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Keywords: tubeworm, last glacial maximum, gas hydrate, vesicomyidae, Annelida, paleobiology, eastern Pacific, methane seep
Citation: Georgieva MN, Paull CK, Little CTS, McGann M, Sahy D, Condon D, Lundsten L, Pewsey J, Caress DW and Vrijenhoek RC (2019) Discovery of an Extensive Deep-Sea Fossil Serpulid Reef Associated With a Cold Seep, Santa Monica Basin, California. Front. Mar. Sci. 6:115. doi: 10.3389/fmars.2019.00115
Received: 01 November 2018; Accepted: 25 February 2019;
Published: 19 March 2019.
Edited by:
Randi D. Rotjan, Boston University, United StatesReviewed by:
Lorenzo Angeletti, Istituto di Scienze Marine (ISMAR), ItalyAmerico Montiel, University of Magallanes, Chile
Copyright © 2019 Georgieva, Paull, Little, McGann, Sahy, Condon, Lundsten, Pewsey, Caress and Vrijenhoek. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Magdalena N. Georgieva, m.georgieva@nhm.ac.uk; magdalena.n.georgieva@gmail.com